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Term:
Parent Terms Term With Siblings Child Terms
arthritis +   
autosomal dominant osteosclerosis, Worth type 
Caffey disease 
Caffey disease is an osteosclerotic dysplasia characterized by acute inflammation with massive subperiosteal new bone formation usually involving the diaphyses of the long bones, as well as the ribs, mandible, scapulae, and clavicles. The disease is associated with fever, irritability pain and soft tissue swelling, with onset around the age of 2 months and resolving spontaneously by the age of 2 years. However, prenatal disease onset has also been described.
chondrodysplasia Blomstrand type 
craniodiaphyseal dysplasia 
desmosterolosis 
diffuse idiopathic skeletal hyperostosis  
dysplastic cortical hyperostosis +  
epicondylitis +  
exostosis +   
hyperostosis corticalis generalisata 
lethal osteosclerotic bone dysplasia 
osteitis deformans +   
osteomyelitis +   
sclerosteosis +  
X-linked calvarial hyperostosis 

Synonyms
Exact Synonyms: cortical congenital hyperostosis ;   infantile cortical hyperostosis
Alternate IDs: MONDO:0007244
Xrefs: DOID:4257 ;   GARD:1051 ;   ICD9:756.59 ;   MEDGEN:43781 ;   MESH:D006958 ;   MIM:114000 ;   NCI:C118423 ;   ORDO:1310 ;   SCTID:24752008 ;   UMLS:C0020497
Definition Sources: Orphanet:1310

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